๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Studies in the tetraarylborates : The preparation and reagent properties of sodium tetrakis(p-chlorophenyl)borate

โœ Scribed by Frank P. Cassaretto; John J. McLafferty; Carl E. Moore

Publisher
Elsevier Science
Year
1965
Tongue
English
Weight
478 KB
Volume
32
Category
Article
ISSN
0003-2670

No coin nor oath required. For personal study only.

๐Ÿ“œ SIMILAR VOLUMES

Studies in the tetraarylborates: Part II
Studies in the tetraarylborates: Part II. The preparation and reagent properties of sodium tetrakis(p-fluorophenyl)borate, a selective reagent for cesium
โœ Carl E. Moore; Frank P. Cassaretto; Harvey Posvic; John J. McLafferty ๐Ÿ“‚ Article ๐Ÿ“… 1966 ๐Ÿ› Elsevier Science ๐ŸŒ English โš– 389 KB

Rcceivcd Octobci gth, 1965) \* !The cleniental analysis of this compound proved very difficult. After some method research, tho Huffman Laboratories, Wheatritlgc, Colorado, were able to report a satisfactory method for the sodium salt. Awl. klrim. A&a, 35 (x966) 'I-5

31P and 23Na NMR studies of the structur
31P and 23Na NMR studies of the structure and lability of the sodium shift reagent, bis(tripolyphosphate)dysprosium(iii) ([dy(p3O10)]7โˆ’) ion, and its decomposition in the presence of rat muscle
โœ N. A. Matwiyoff; C. Gasparovic; R. Wenk; J. D. Wicks; A. Rath ๐Ÿ“‚ Article ๐Ÿ“… 1986 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 263 KB

The 31P NMR of aqueous [Dy(P3O10)2]7- demonstrates that it is in slow exchange with P3O5-10 on the NMR time scale. In the presence of tissue, [Dy(P3O10)2]7- decomposes to PO4 with an accompanying slow change of the tissue 23Na NMR of extracellular Na+ ion in several NMR distinguishable extracellular

ChemInform Abstract: Diastereoselective
ChemInform Abstract: Diastereoselective Reaction of a Grignard Reagent with Chiral Imides: A Practical Preparation of a Key Intermediate in the Synthesis of Ifetroban Sodium.
โœ R. H. MUELLER; S. WANG; P. D. PANSEGRAU; J. Q. JANNOTTI; M. A. POSS; J. K. THOTT ๐Ÿ“‚ Article ๐Ÿ“… 2010 ๐Ÿ› John Wiley and Sons โš– 32 KB ๐Ÿ‘ 2 views

Diastereoselective Reaction of a Grignard Reagent with Chiral Imides: A Practical Preparation of a Key Intermediate in the Synthesis of Ifetroban Sodium. -The synthesis of the key intermediate (VIII) of ifetroban sodium is achieved via efficient formation of the chiral imine (IV) and its diastereose